Target intelligence / Profile preview

PAXIP1 antisense RNA 2 (PAXIP1-AS2)

Target
PAXIP1-AS2
Molecular classification
Long non-coding RNA (lncRNA), Antisense RNA
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Overview

PAXIP1 antisense RNA 2 (PAXIP1-AS2) is a long non-coding RNA transcribed antisense to the PAXIP1 gene. It modulates the translesion DNA synthesis (TLS) pathway by influencing the expression of regulatory proteins including RAD18 and DNA polymerase η, thus affecting how cells tolerate and repair DNA damage. Overexpression of PAXIP1-AS2 or knockdown of related proteins (such as TENT4A or CYLD) leads to decreased levels of RAD18 and DNA polymerase η, consequently reducing TLS efficiency. Dysregulation of TLS-regulating genes, including PAXIP1-AS2 and its network, is frequently observed in endometrial cancer genomes and may contribute to cancer progression by promoting genomic instability. PAXIP1-AS2 is not a protein or classical receptor, but an antisense lncRNA that exerts its effects at the transcriptional and post-transcriptional level, providing a potential target for future therapeutic approaches and biomarker development in oncology.

02

Mechanism of action

For experimental modulation: Overexpression or knockdown of PAXIP1-AS2 alters DNA repair/tolerance via the TLS pathway. Not applicable for drugs, since no direct drug interventions reported.

03

Biological functions

Regulation of translesion DNA synthesis (TLS)Modulation of DNA damage toleranceRegulation of RAD18 and DNA polymerase η protein levels
04

Disease associations

Cancer (notably endometrial cancer)Possibly other malignancies (pending further research)
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Safety considerations

No specific safety concerns or therapeutic challenges documented for direct targeting (as no drugs currently exist); general challenges would include lncRNA targeting specificity and delivery
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Biomarkers

Abnormal expression of PAXIP1-AS2 may serve as a biomarker for TLS dysregulation in endometrial cancerCould potentially serve as a biomarker for DNA damage tolerance states in tumors; not yet established clinically

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